Euroopa Liit - eesti - EMA (European Medicines Agency)

sanofi winthrop industrie - klopidogreeli vesiniksulfaat - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - antitrombootilised ained - secondary prevention of atherothrombotic eventsclopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from seven days until less than six months) or established peripheral arterial disease;adult patients suffering from acute coronary syndrome:non-st-segment-elevation acute coronary syndrome (unstable angina or non-q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa);st-segment-elevation acute myocardial infarction, in combination with asa in patients undergoing percutaneous coronary intervention (including patients undergoing a stent replacement) or medically treated patients eligible for thrombolytic/fibrinolytic therapy. in patients with moderate to high-risk transient ischemic attack (tia) or minor ischemic stroke (is)clopidogrel in combination with asa is indicated in:adult patients with moderate to high-risk tia (abcd2  score ≥4) or minor is (nihss  ≤3) within 24 hours of either the tia or is event. ennetamine atherothrombotic ja trombembooliliste sündmuste kodade fibrillationin täiskasvanud patsientidel, kellel on kodade virvendus, kes on vähemalt üks riskifaktor veresoonkonna sündmused, ei sobi ravi koos vitamiin-k antagonistid ja kes on vähese verejooksu riski, clopidogrel on näidustatud kombinatsioonis asa ennetamise atherothrombotic ja trombembooliliste sündmuste, sealhulgas insult.

Euroopa Liit - eesti - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - nivolumab, relatlimab - melanoom - antineoplastic agents, monoclonal antibodies - opdualag is indicated for the first line treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older with tumour cell pd l1 expression < 1%.

Euroopa Liit - eesti - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - deucravacitinib - psoriaas - immunosupressandid - treatment of moderate-to-severe plaque psoriasis in adults.

Eesti - eesti - Ravimiamet

glaxosmithkline dungarvan limited - terbinafiin - geel - 10mg 1g 15g 1tk

Eesti - eesti - Ravimiamet

orifarm healthcare a/s - hüdrokortisoon - salv - 10mg 1g 30g 1tk; 10mg 1g 10g 1tk

Eesti - eesti - Ravimiamet

aurobindo pharma limited - metformiin - õhukese polümeerikattega tablett - 1000mg 90tk; 1000mg 180tk; 1000mg 50tk; 1000mg 60tk; 1000mg 100tk; 1000mg 20tk; 1000mg 70tk; 1000mg 40tk; 1000mg 80tk

Eesti - eesti - Ravimiamet

aurobindo pharma limited - metformiin - õhukese polümeerikattega tablett - 850mg 90tk; 850mg 56tk; 850mg 180tk; 850mg 200tk; 850mg 60tk; 850mg 30tk; 850mg 100tk; 850mg 70tk; 850mg 500tk; 850mg 120tk; 850mg 50tk; 850mg 42tk; 850mg 20tk

Eesti - eesti - Ravimiamet

aurobindo pharma limited - metformiin - õhukese polümeerikattega tablett - 500mg 28tk; 500mg 400tk; 500mg 500tk; 500mg 84tk; 500mg 60tk; 500mg 30tk; 500mg 50tk; 500mg 90tk; 500mg 98tk; 500mg 70tk; 500mg 42tk; 500mg 300tk; 500mg 56tk; 500mg 200tk; 500mg 20tk; 500mg 100tk; 500mg 40tk

Euroopa Liit - eesti - EMA (European Medicines Agency)

viiv healthcare bv - lamivudine, zidovudine - hiv-nakkused - viirusevastased ravimid süsteemseks kasutamiseks - combivir is indicated in antiretroviral combination therapy for the treatment of human immunodeficiency virus (hiv) infection.

Euroopa Liit - eesti - EMA (European Medicines Agency)

laboratoire hra pharma - ulipristaal - kontraceptsioon, postkoital - suguhormoonid ja genitaalsüsteemi, , hädaabi rasestumisvastased vahendid - hädaabi kontratseptsioon 120 tundi (5 päeva) rasestumisvastaseid vahendeid või kaitsmata seksuaalvahekorras.